2020
DOI: 10.1016/j.solener.2020.03.035
|View full text |Cite
|
Sign up to set email alerts
|

Highly thermally stable all-polymer solar cells enabled by photo-crosslinkable bromine-functionalized polymer donors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
10
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 13 publications
(10 citation statements)
references
References 49 publications
0
10
0
Order By: Relevance
“…In our previous work, we found that increasing the amount of the D (BDT-T) unit would weaken the push-pull interaction of the D-A unit and reduce the degree of crystalline behaviour, which is advantageous for the complementary absorption and miscibility of the crystalline acceptors. Herein, we report D-A-type random bi-polymers (PBDT a -TPD b ) 47 and D-D 1 -D-A type terpolymers (PBDT(T)FTAZ-B n ) 48 with obviously enhanced J SC and PCE values by simply tuning the D-A molar ratio. Very recently, non-equivalent D-A copolymer donors (PM6-Dn) with an enhanced performance were reported by Li's group, indicating that increasing the D-A molar ratio is an effective strategy resulting in random copolymerization.…”
Section: Introductionmentioning
confidence: 99%
“…In our previous work, we found that increasing the amount of the D (BDT-T) unit would weaken the push-pull interaction of the D-A unit and reduce the degree of crystalline behaviour, which is advantageous for the complementary absorption and miscibility of the crystalline acceptors. Herein, we report D-A-type random bi-polymers (PBDT a -TPD b ) 47 and D-D 1 -D-A type terpolymers (PBDT(T)FTAZ-B n ) 48 with obviously enhanced J SC and PCE values by simply tuning the D-A molar ratio. Very recently, non-equivalent D-A copolymer donors (PM6-Dn) with an enhanced performance were reported by Li's group, indicating that increasing the D-A molar ratio is an effective strategy resulting in random copolymerization.…”
Section: Introductionmentioning
confidence: 99%
“…Organic solar cells (OSCs) based on polymer acceptors attract considerable attention for potential commercial application because of their superior thermal and light stability, and excellent efficiency. 1–11 The energy loss for the polymer acceptor could also be as low as 0.47 eV. 6,8 Importantly, the polymer acceptor could be easily polymerized from the small acceptors, and their opto-electrical properties could be well tuned through the monomer or ternary copolymerization.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, another study fabricated an active layer using a crosslinkable thieno­[3,4- c ]­pyrrole-4,6-dione­(TPD) donor polymer and IT-4F acceptor, and the corresponding PSC with this active layer achieved a PCE of 12.18% . Ling et al fabricated all-PSCs using a blend film of a 4,7-bis­(thiophen-2-yl)­benzo­[ c ]­[1,2,5]­thiadiazole-based crosslinkable donor and N2200 acceptor polymer. The PSCs bearing the crosslinked active layer achieved a PCE of 7.21% of and exhibited excellent thermal stability …”
Section: Introductionmentioning
confidence: 99%
“…Ling et al fabricated all-PSCs using a blend film of a 4,7-bis­(thiophen-2-yl)­benzo­[ c ]­[1,2,5]­thiadiazole-based crosslinkable donor and N2200 acceptor polymer. The PSCs bearing the crosslinked active layer achieved a PCE of 7.21% of and exhibited excellent thermal stability …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation